Evidence map›Paper›PMID 33824385›Full record

ArticleScientific reports2021

Identification of PDGFRα-positive interstitial cells in the distal segment of the murine vas deferens.

Tasuku Hiroshige, Kei-Ichiro Uemura, Shingo Hirashima, Kiyosato Hino, Akinobu Togo, Keisuke Ohta, Tsukasa Igawa, Kei-Ichiro Nakamura

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Telocytes inside of the peripheral nervous system - a 3D endoneurial network and putative role in cell communication.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Tasuku HiroshigeDivision of Microscopic and Development Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan. hiroshige_tasuku@med.kurume-u.ac.jp.
Kei-Ichiro UemuraDepartment of Urology, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Shingo HirashimaDivision of Microscopic and Development Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Kiyosato HinoDivision of Microscopic and Development Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Akinobu TogoAdvanced Imaging Research Center, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Keisuke OhtaDivision of Microscopic and Development Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Tsukasa IgawaDepartment of Urology, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Kei-Ichiro NakamuraDivision of Microscopic and Development Anatomy, Department of Anatomy, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Kurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platelet-derived growth factor receptor-α (PDGFRα)-positive interstitial cells (ICs) are widely distributed in various organs and may be involved in the motility of various tubular organs. We, for the first time, aimed to investigate the distribution, immunohistochemical characteristics, and ultrastructure of PDGFRα-positive ICs in murine vas deferens, using confocal laser scanning microscopy, transmission electron microscopy (TEM), and immuno-electron microscopy (immuno-EM). For immunofluorescence, we used antibodies against PDGFRα and other markers of ICs. PDGFRα-positive ICs were distributed widely in the lamina propria, smooth muscles, and serosal layers. Although most PDGFRα-positive ICs labeled CD34, they did not label CD34 in the subepithelial layers. Additionally, PDGFRα-positive ICs were in close proximity to each other, as also to the surrounding cells. TEM and immuno-EM findings revealed that PDGFRα-positive ICs established close physical interactions with adjacent ICs. Extracellular vesicles were also detected around the PDGFRα-positive ICs. Our morphological findings suggest that PDGFRα-positive ICs may have several subpopulations, which can play an important role in intercellular signaling via direct contact with the IC network and the extracellular vesicles in the murine vas deferens. Further investigation on PDGFRα-positive ICs in the vas deferens may lead to understanding the vas deferens mortility.

Indexed as

AnimalsHumansInterstitial Cells of CajalMaleMiceMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalMuscle, SmoothReceptor, Platelet-Derived Growth Factor alphaVas DeferensReceptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID33824385
PMCPMC8024294
OpenAlexW3149626237

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.